rs113994133

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs113994133(A;G)

Make rs113994133(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

99916587

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs113994133
dbSNP (classic)	rs113994133
ClinGen	rs113994133
ebi	rs113994133
HLI	rs113994133
Exac	rs113994133
Gnomad	rs113994133
Varsome	rs113994133
LitVar	rs113994133
Map	rs113994133
PheGenI	rs113994133
Biobank	rs113994133
1000 genomes	rs113994133
hgdp	rs113994133
ensembl	rs113994133
geneview	rs113994133
scholar	rs113994133
google	rs113994133
pharmgkb	rs113994133
gwascentral	rs113994133
openSNP	rs113994133
23andMe	rs113994133
SNPshot	rs113994133
SNPdbe	rs113994133
MSV3d	rs113994133
GWAS Ctlg	rs113994133

Max Magnitude

0

OMIM	610860
Desc
Variant	0006
Related	also

ClinVar
Risk	rs113994133(G;G)
Alt	rs113994133(G;G)
Reference	Rs113994133(A;A)
Significance	Pathogenic
Disease	Glycogen storage disease IIIb Glycogen storage disease IIIa Glycogen storage disease type III
Variation	info
Gene	LOC101930120 AGL
CLNDBN	Glycogen storage disease IIIb Glycogen storage disease IIIa Glycogen storage disease type III
Reversed	0
HGVS	NC_000001.11:g.99916398A>G
CLNSRC	GeneReviews OMIM Allelic Variant
CLNACC	RCV000001157.2, RCV000001158.2, RCV000020379.1,